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The Clinical Documentation Specialist performs record review (quantitative and qualitative) and assesses the level of compliance with stated regulatory requirements by area of job focus.
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Leads all regulatory compliance reviews for new product launches in accordance with brand specific blacklist and international distribution list – including but not limited to retailer requirements (Ulta, Beauty Bay and more) and regional specific requirements (U.S., Canada, EU/UK, Australia, APAC and more.
$130,000 - $150,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The School and its faculty uniquely spans the entire spectrum of pharmaceutical development and clinical care from drug discovery to regulatory approaches that promote safety and innovation, from delivery of patient care services to evaluating the impact of care on patient outcomes and costs.
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Whether your project is a low or high-rise office building, a shopping mall, hospital, semi-conductor fabrication facility or pharmaceutical manufacturing plant. Whether your project is a low or high-rise office building, a shopping mall, hospital, semi-conductor fabrication facility, or pharmaceutical manufacturing plant.
$51.69 - $62.55 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Manager of Quality and Compliance is responsible for leading and maintaining the regulatory compliance and process improvement initiatives of the transplant institute as set by the Organ Procurement Transplant Network (OPTN) / United Network for Organ Sharing (UNOS), CMS, Joint Commission, Intermacs, and the ESRD Network.
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Stantec is seeking a Senior Scientist/Environmental Engineer/Safety Professional to lead a team of EHS professionals/EHS compliance specialists delivering EHS and sustainability solutions to commercial, pharmaceutical, food and beverage, manufacturing, mining, oil and gas, power, and other industrial clients.
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Evaluating the performance of investment portfolios and ensuring compliance with standards provided by regulatory organizations, including conformance with investor disclosures, privacy laws, anti-money laundering requirements, and anti-fraud measures.
$140,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Minimum 10 years of previous experience working in HEOR and/or RWE outcomes research in the pharmaceutical, managed care or consulting industries.
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In this dynamic role, you'll oversee construction activities on behalf of our clients, diligently monitoring contractor regulatory and contract safety compliance. Possess at least five years of in-depth familiarity with DSA regulations, ensuring compliance and safety across the board.
$95,000 - $105,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Oversee all affordable compliance and regulatory reporting requirements. The Affordable Housing Compliance Specialist will be responsible for supporting the Asset Management team in the day-to-day administration of all Asset Management projects, policies, and procedures with a specific focus on managing all affordable compliance and reporting for BLVD’s affordable portfolio consisting of both Section 8 and LIHTC properties.
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The candidate will embark on developing pioneering micro-organoid and organ-on-a-chip technology to improve ongoing precision medicine clinical trials, under the guidance of the Chief Scientific Officer Dr. Xiling Shen and the Director of Precision Medicine Dr. Zhaohui Wang. TIBI's mission revolves around personalized diagnostics and therapeutics, collaborating closely with clinicians, biotech companies, and pharmaceutical partners to transform patient care.
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Founded in 1981, Analysis Group is one of the largest international economics consulting firms, with more than 1,200 professionals across 14 offices, including more than 250 professionals who focus on Health Care. Analysis Group’s health care experts apply analytical expertise to health economics and outcomes research (HEOR), clinical research, market access and commercial strategy, health care policy, epidemiology and drug safety, data science, and biostatistics.
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Perform work in compliance with Lilly Research Labs policies. RequirementsUndergraduate degree in chemistry or a closely related field with laboratory research experienceAt least 1 year of experience designing, validating, performing, and analyzing experiments to generate synthetic compounds of interest.
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Assist LACMTA's Environmental Compliance and Services Department in regulatory compliance, including but not limited to stormwater management, environmentally related permitting, and environmental mitigation monitoring.
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The hematology team providers are recognized for their range of clinical, teaching, research, and clinical trial achievements. This position will involve clinical practice in non-malignant hematology as well as clinical, academic (research and/or education), and administrative responsibilities.
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clinical research pharmaceutical company regulatory compliance jobs Title: senior director in Los Angeles, CA
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